4.8 Article

A Gold(III) Porphyrin Complex with Antitumor Properties Targets the Wnt/beta-catenin Pathway

Journal

CANCER RESEARCH
Volume 70, Issue 1, Pages 329-337

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-09-3324

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Funding

  1. University of Hong Kong
  2. Hong Kong Research Grant Council [HKU 777908M, HKU 779707M]
  3. University Grants Committee HKSAR

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Gold(III) complexes have shown promise as antitumor agents, but their clinical usefulness has been limited by their poor stability under physiological conditions. A novel gold(III) porphyrin complex [5-hydroxyphenyl-10,15,20-triphenylporphyrinato gold(III) chloride (gold-2a)] with improved aqueous stability showed 100-fold to 3,000-fold higher cytotoxicity than platinum-based cisplatin and IC(50) values in the nanomolar range in a panel of human breast cancer cell lines. Intraductal injections of gold-2a significantly suppressed mammary tumor growth in nude mice. These effects are attributed, in part, to attenuation of Wnt/beta-catenin signaling through inhibition of class I histone deacetylase (HDAC) activity. These data, in combination with computer modeling, suggest that gold-2a may represent a promising class of anticancer HDAC inhibitor preferentially targeting tumor cells with aberrant Wnt/beta-catenin signaling. Cancer Res; 70(1); 329-37. (C)2010 AACR.

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